Manager, Clinical Supplies Production

At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science.In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.


  • Demonstrates a thorough working knowledge of the clinical supply process and the technical aspects of the CGMP’s as they relate to product packaging and labeling. Applies this knowledge to day-to-day packaging and labeling activities that produce finished packaged clinical supplies while ensuring and maintaining compliance with all quality requirements.
  • Reviews the master production schedule and production orders, establishes priorities and revises schedules according to production order specifications, established priorities and availability of workers, materials and equipment.
  • Exhibits sound judgment and strong supervisory skills by executing shop floor orders against required timelines while utilizing shop floor resources in an optimized efficient and cost-effective manner.
  • Supervises union staff in all aspects of packaging and labeling of clinical supplies.
  • Maintain employee records (attendance, vacation etc.) and conduct performance reviews of Hourly staff.
  • Assures all production orders are executed in accordance with CGMP's and departmental SOP's.
  • Utilizing SAP, d elivers complete, error free technical documentation supporting packaging & labeling and label inspection production processes .
  • Demonstrates knowledge and familiarity with a range of production equipment and can independently troubleshoot and resolve problems as they arise.
  • Develops and recommends improvements to facilities, equipment or procedures to improve quality, safety, and efficiency.
  • Establish and support a work environment of continuous improvements that supports the Company’s Quality policy, Quality Systems and the appropriate regulations for the area.
  • Utilizes technical writing skills to generate procedures and guidelines.
  • Participates on high performing teams representing global packaging organization as subject matter expert.
  • Interacts and liaises with team members from CSO, Quality and Analytical & Bioanalytical Development.
  • Oversees and or conducts training of new or existing employees and ensures their training is documented.
  • Ensures that health and safety guidelines are followed. Maintains CGMP/Housekeeping at a high level within the department.
  • Leads root cause investigations for process deviations and assigns Corrective/Preventative Actions.

Education/Experience Requirements:
  • Bachelors of Science or a Mechanical Engineering Degreeis required.
  • 5+ Years in a pharmaceutical industry preferably pharmaceutical manufacturing with a focus in the production of Clinical Trial Supplies is preferred.
  • 3-5 years of progressive leadership or supervisory experience in the pharmaceutical industry is required.
  • Working knowledge and experience in lean /six sigma tools and concepts; 5S, Kanban, Kaizen, Green Belt Black Belt, etc.
  • Prior Supervision of production staff or leadership role within a production operation with demonstrated ability in scheduling, organizing and team building is required.
  • Strong working knowledge of cGMP’s and regulatory (i.e. FDA, EU, OSHA, etc) requirements and their application within a packaging and labeling production environment. Solid record of attention to detail and strict adherence to all procedures and regulations.
  • Good understanding of the pharmaceutical development process and associated scientific principles,
  • Excellent written and communication skills. Demonstrated ability to liaise with various support groups and lead in a team environment.
  • Effectively manage competing priorities, adaptable to change, demonstrated ability to accept additional responsibilities and mange tasks thought teamwork.
  • Basic working knowledge of computers using MS Office, MS

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives.

Our company is committed to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace adjustments and ongoing support in their roles. Applicants can request an approval of accommodation prior to accepting a job offer. If you require reasonable accommodation in completing this application, or any part of the recruitment process direct your inquiries to Visit to access our complete Equal Employment Opportunity statement.